Article ID Journal Published Year Pages File Type
1365557 Bioorganic & Medicinal Chemistry Letters 2007 5 Pages PDF
Abstract

A series of compounds originally derived from thalidomide were synthesized and evaluated. The most potent compounds in this series, 5HPP-33 and compound 20, inhibited NF-κB activation in HeLa cells. Preliminary study indicated that the mechanism of inhibition of NF-κB activation is through inhibition of its translocation from the cytoplasm to the nucleus.

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Physical Sciences and Engineering Chemistry Organic Chemistry
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